|
NM_021939.4:c.829C>G
MANE Select
|
NP_068758.3:p.Pro277Ala
|
|
ENST00000321562.9:c.829C>G
MANE Select
|
ENSP00000317232.4:p.Pro277Ala
|
|
NM_021939.3:c.829C>G , LRG_12t1:c.829C>G
|
NP_068758.3:p.Pro277Ala
|
|
ENST00000321562.8:c.829C>G
|
ENSP00000317232.4:p.Pro277Ala
|
|
ENST00000455106.1:c.57C>G
|
|
|
ENST00000487489.1:n.442C>G
|
|
|
ENST00000489591.5:c.*239C>G
|
ENSP00000466352.1:n.*239C>G
|
|
ENST00000706683.1:c.727+784C>G
|
ENSP00000516497.1:n.727+784C>G
|
|
XM_011525099.1:c.829C>G
|
XP_011523401.1:p.Pro277Ala
|
|
XM_011525099.3:c.829C>G
|
XP_011523401.1:p.Pro277Ala
|
|
XM_011525100.1:c.556C>G
|
XP_011523402.1:p.Pro186Ala
|
|
XM_011525100.2:c.556C>G
|
XP_011523402.1:p.Pro186Ala
|